Faculty & Research > Faculty > W. Dean Harman, Chair

Harman, Dean

W. Dean Harman, Chair

Professor of Chemistry

wdh5z@virginia.edu
Room 404, Chemistry Building (434) 924-3060

Harman Group Website

B. Sc. Stanford University, 1983

Ph. D. Stanford University, 1987

Research Associate, Stanford University, 1988-89

For decades, the dearomatization of arenes has been recognized as a chemical transformation of fundamental importance. It provides the connection between this robust and abundant source of hydrocarbons and the alicyclic frameworks common to many biologically active products. Thus, dearomatization methods have become powerful tools for organic synthesis.

The chemical properties of arenes are influenced by their coordination to a transition metal. For example, complexes such as (η6-arene)Cr(CO)3+ and its cationic analogs (e.g., FeCp+, RuCp+, Mn(CO)3+) are susceptible to nucleophilic substitution or addition, ultimately leading to the formation of substituted arenes or cyclohexadienes, respectively. During the past three decades, the application of η6-arene complexes to organic synthesis has been widely explored.

In the Harman Research Group, an alternative approach to the dearomatization of arenes has been developed in which the aromatic system may be activated toward organic transformations by η2-coordination. Here, the metal-arene bond is stabilized primarily by the interaction of filled metal dπorbitals with the  π* system of the arene, an interaction having two important consequences for the activation of the aromatic ring. Through πbackbonding, the aromatic π system becomes more electron-rich, similar to what is observed for organic arenes bearing electron-donating groups. Additionally, structural data for complexes containing η2-coordinated aromatic rings show significant distortions in the bond lengths of the ring consistent with a localization of πelectron density. Together, these effects activate η2-bound aromatic systems toward electrophilic rather than nucleophilic addition. When the π base binds an aromatic heterocycle such as a pyridine, furan or pyrrole, novel tandem addition reactions and cycloaddition reactions become possible.

Of the handful of transition metal systems that are known to form stable η2 complexes with aromatic molecules, only d6 octahedral metal complexes have been shown to enhance the reactivity of the aromatic ligand toward electrophiles to date. For nearly a decade, despite our best efforts, this mode of arene activation was known only for the pentaammineosmium(II) system. However, in the past few years a new generation of dearomatization agents have been developed in our group based on a careful matching of the d5/d6 reduction potential of rhenium(I), tungsten(0), and molybdenum(0) complexes with that of pentaammineosmium(II).

Recent Publications

[4 + 2] Cyclocondensation reactions of tungsten-dihydropyridine complexes and the generation of tri- and tetrasubstituted piperidines. Harrison DP, Iovan DA, Myers WH, Sabat M, Wang S, Zottig VE, Harman WD. J Am Chem Soc. 133:18378-87 (2011).

Polarization of the pyridine ring: highly functionalized piperidines from tungsten-pyridine complex. Harrison DP, Sabat M, Myers WH, Harman WD. J Am Chem Soc. 132:17282-95 (2010).

Efficient synthesis of an eta2-pyridine complex and a preliminary investigation of the bound heterocycle’s reactivity. Harrison DP, Welch KD, Nichols-Nielander AC, Sabat M, Myers WH, Harman WD. J Am Chem Soc. 130:16844-5 (2008).

Synthesis of 1-oxadecalins from anisole promoted by tungsten. Lis EC Jr, Salomon RJ, Sabat M, Myers WH, Harman WD. J Am Chem Soc. 130:12472-6 (2008).

Stereoselective umpolung tandem addition of heteroatoms to phenol. Todd MA, Sabat M, Myers WH, Smith TM, Harman WD.
J Am Chem Soc. 130:6906-7 (2008).

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